Neural crest migration and mouse models of congenital heart disease

Cold Spring Harb Symp Quant Biol. 2002:67:57-62. doi: 10.1101/sqb.2002.67.57.
No abstract available

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.
  • Review

MeSH terms

  • Animals
  • Carrier Proteins / genetics
  • Cell Movement
  • DNA-Binding Proteins / genetics
  • DiGeorge Syndrome / embryology
  • DiGeorge Syndrome / genetics
  • Disease Models, Animal
  • Double Outlet Right Ventricle / embryology
  • Double Outlet Right Ventricle / genetics
  • Genes, Neurofibromatosis 1
  • Heart Defects, Congenital / embryology*
  • Heart Defects, Congenital / genetics*
  • Humans
  • Mice
  • Mutation
  • Nerve Tissue Proteins / deficiency
  • Nerve Tissue Proteins / genetics
  • Neural Crest / cytology
  • Neural Crest / embryology*
  • PAX3 Transcription Factor
  • Paired Box Transcription Factors
  • Semaphorin-3A*
  • T-Box Domain Proteins / genetics
  • Transcription Factors*

Substances

  • Carrier Proteins
  • DNA-Binding Proteins
  • Nerve Tissue Proteins
  • PAX3 Transcription Factor
  • PAX3 protein, human
  • Paired Box Transcription Factors
  • SEMA3A protein, human
  • Sema3a protein, mouse
  • Semaphorin-3A
  • T-Box Domain Proteins
  • TBX1 protein, human
  • Tbx1 protein, mouse
  • Transcription Factors
  • Pax3 protein, mouse